Cleared Traditional

Disposable Endoscopy Valve Set

K250732 · Yangzhou Fartley Medical Instrument Technology Co., Ltd. · Gastroenterology & Urology
Jun 2025
Decision
101d
Days
Class 2
Risk

About This 510(k) Submission

K250732 is an FDA 510(k) clearance for the Disposable Endoscopy Valve Set, a Endoscope Channel Accessory (Class II — Special Controls, product code ODC), submitted by Yangzhou Fartley Medical Instrument Technology Co., Ltd. (Yangzhou, CN). The FDA issued a Cleared decision on June 20, 2025, 101 days after receiving the submission on March 11, 2025. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K250732 FDA.gov
FDA Decision Cleared SESE
Date Received March 11, 2025
Decision Date June 20, 2025
Days to Decision 101 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code ODC — Endoscope Channel Accessory
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Give The Endoscope Channel Additional Or Improved Functionality.

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